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Plain-language summaries of 10,888 rare conditions, drawn from MONDO, GeneReviews, ClinVar, FDA, NIH, ClinicalTrials.gov, PubMed, and 5 other public sources. Free, sourced, never gated.
Kisho provides public health information only — not medical advice. Always consult your healthcare provider.
12
authoritative sources — clinical, regulatory, scientific
10,888
rare conditions, continuously monitored
Daily
updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…
Showing 3,301-3,320 of 10,888 diseases
MONDO:0009813
Chronic recurrent multifocal osteomyelitis, also known as chronic nonbacterial osteomyelitis (CNO) or CRMO, is a chronic autoinflammatory condition ch...
MONDO:0958177
Chronic recurrent multifocal osteomyelitis 3 is an inherited disorder that primarily affects the skeletal system, leading to repeated episodes of bone...
MONDO:0044687
Chronic relapsing inflammatory optic neuropathy is a rare condition that involves inflammation of the optic nerves, leading to severe and persistent o...
MONDO:0016323
Chronic respiratory distress with surfactant metabolism deficiency is a condition affecting the respiratory system, leading to ongoing difficulties wi...
MONDO:0013024
Chronic thromboembolic pulmonary hypertension (CTEPH) is a condition in which organized thromboembolic material obstructs the pulmonary arteries, lead...
MONDO:0004372
Chronic toxic polyneuropathy is a condition characterized by long-term nerve damage, typically affecting the peripheral nerves. The condition does not...
MONDO:0011411
Chudley-McCullough syndrome is a rare condition that has been documented in genetic and medical databases. It is known by several names including CMCS...
MONDO:0009892
Chuvash polycythemia is a rare genetic condition present from birth. It is characterized by higher than normal levels of hemoglobin, hematocrit, and e...
MONDO:0007327
Familial chylomicronemia due to circulating inhibitor of lipoprotein lipase is a condition affecting lipid metabolism and the body’s ability to proper...
MONDO:0009528
Chylomicron retention disease is a familial condition characterized by impaired lipid absorption, leading to malnutrition and multiple organ complicat...
MONDO:0008829
Chylous ascites is a rare condition characterized by the accumulation of lymph in the peritoneal cavity, leading to abdominal distension. It is most o...
MONDO:0014098
CIDEC-related familial partial lipodystrophy is a rare form of lipodystrophy that has been linked to mutations in the CIDEC gene. This condition is re...
MONDO:0004086
Ciliary body epithelioid cell melanoma is a malignant tumor of the eye that arises in the ciliary body, a part of the uveal tract. This condition is d...
MONDO:0003911
Ciliary body mixed cell melanoma is a type of uveal melanoma that arises from the ciliary body of the eye. As an ocular malignancy, it involves a mixt...
MONDO:0003746
Ciliary body spindle cell melanoma is a malignant tumor originating in the spindle cells of the ciliary body of the eye. As an ocular melanoma, it aff...
MONDO:0008984
Ciliary discoordination due to random ciliary orientation is a condition affecting the coordinated movement of cilia in the body. The precise genetic...
MONDO:0010517
ciliary dyskinesia, primary, 36, X-linked is a condition affecting the respiratory system that impairs the normal movement of cilia, which help clear...
MONDO:0033204
Ciliary dyskinesia, primary, 37 is a condition that affects the structure and function of cilia, the tiny hair-like projections that play a critical r...
MONDO:0054843
Ciliary dyskinesia, primary, 38 is a condition that affects the respiratory system through dysfunction of small, hair-like structures called cilia. Va...
MONDO:0032637
Ciliary dyskinesia, primary, 39 is a condition that primarily affects the respiratory system and the function of cilia, the tiny hair-like structures...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.